Bethyl will be closed Monday, May 28th in observance of Memorial Day and will resume normal business hours on Tuesday, May 29th. Thank you!

Aprataxin Antibody

The Aprataxin gene was identified by linkage analysis as the defective gene in the neurogenerative disorder ataxia with oculomotor apraxia type 1 (AOA1) which is characterized by cerebellar ataxia, peripheral neuropathy, and hypoalbuminemia. Aprataxin functions in the DNA damage response and is involved in single-strand and double-strand break repair, and base excision repair.
APTX
aprataxin
Aprataxin
:  AOA AOA1 ataxia 1, early onset with hypoalbuminemia AXA1 EAOH EOAHA FHA-HIT FLJ20157 forkhead-associated domain histidine triad-like protein
Product
Specifications
Ordering Information
Human
WB, IP
Between 100 and 150
This item is backordered. Please contact Bethyl Customer Support at 1-800-338-9579 if you are interested in purchasing this item. Expected Release late June 2018 (Updated 05/18/2018)
This item is backordered. Please contact Bethyl Customer Support at 1-800-338-9579 if you are interested in purchasing this item. Expected Release late June 2018 (Updated 05/18/2018)
This item is backordered. Please contact Bethyl Customer Support at 1-800-338-9579 if you are interested in purchasing this item. Expected Release late June 2018 (Updated 05/18/2018)